Spongy Diamond
M.
Diudea
Babes-Bolyai University, Cluj, Romania
author
M.
Medeleanu
University of Politehnica, Timisoara, Romania
author
Z.
Khalaj
Shahr-e-Qods Branch, Islamic Azad University, Tehran, Iran
author
A.
Ashrafi
University of Kashan
author
text
article
2019
eng
Rhombellanes are mathematical structures existing in various environments, in crystal or quasicrystal networks, or even in their homeomorphs, further possible becoming real molecules. Rhombellanes originate in the K2.3 complete bipartite graph, a tile found in the linear polymeric staffanes. In close analogy, a rod-like polymer derived from hexahydroxy-cyclohexane was imagined. Further, the idea of linear polymer synthesized from dehydro-adamantane was extended in the design of a three-dimensional crystal network, named dia(s), of which tile is a hyper-adamantane (an adamantane of which vertices are just adamantanes). It was suggested that this network could be synthesized starting from the real molecule tetrabromo-adamantane, by dehydrogenation and polymerization. The crystal structures herein proposed were characterized by connectivity and ring surrounding sequences and also by the Omega polynomial.
Iranian Journal of Mathematical Chemistry
University of Kashan
2228-6489
10
v.
1
no.
2019
1
9
http://ijmc.kashanu.ac.ir/article_81623_4cf12483fa350a5ab37df70041109718.pdf
dx.doi.org/10.22052/ijmc.2019.167340.1416
On the Eigenvalues of Rhomboidal C4C8(R)[n; n] Nanotori
F.
Afshari
Department of Mathematics, Karaj Branch, Islamic Azad University, Karaj, Iran
author
M.
Maghasedi
Department of Mathematics, Karaj Branch, Islamic Azad University, Karaj, Iran
author
text
article
2019
eng
A C4C8 net is a trivalent decoration made by alternating squares C4 and octagons C8. It can cover either a cylinder or a torus. In this paper, we study the adjacency spectrum of rhomboidal C4C8 tori. We also give lower and upper bounds for a chemical quantity, namely Estrada index, for a C4C8 net.
Iranian Journal of Mathematical Chemistry
University of Kashan
2228-6489
10
v.
1
no.
2019
11
20
http://ijmc.kashanu.ac.ir/article_87311_183bf9be3b6f035b1a2846a3af2240e1.pdf
dx.doi.org/10.22052/ijmc.2018.118152.1343
Neonicotinoids activity against Cowpea aphids by computational estimation
L.
Crisan
“Coriolan Dragulescu“ Institute of Chemistry, Romanian Academy, Bul. Mihai
Viteazu 24, 300223 Timisoara, Romania
author
A.
Borota
“Coriolan Dragulescu“ Institute of Chemistry, Romanian Academy, Bul. Mihai
Viteazu 24, 300223 Timisoara, Romania
author
A.
Bora
“Coriolan Dragulescu“ Institute of Chemistry, Romanian Academy, Bul. Mihai
Viteazu 24, 300223 Timisoara, Romania
author
S.
Funar-Timofei
“Coriolan Dragulescu“ Institute of Chemistry, Romanian Academy, Bul. Mihai
Viteazu 24, 300223 Timisoara, Romania
author
text
article
2019
eng
In this study, the insecticidal activity against Cowpea aphids (Aphis craccivora) of a series of 23 phenylazo, pyrrole-, dihydropyrrole-fused and chain-opening nitromethyleneneonicotinoids was evaluated by using the multiple linear regression (MLR) and pharmacophore modelling. Conformer insecticide ensembles were modeled using the MMFF94s force field. Minimum energy conformers were employed to calculate structural parameters, which were related to the experimental pLC50 values. Several statistical criteria of goodness of fit and predictivity were checked to validate the models. Robust and predictable MLR models were obtained. Further, the Phase module from Schrodinger suite was engaged in the generation of the ligand-based pharmacophore models. The atom-based 3D-QSAR module from the aforementioned software was used for the validation of a best four-point pharmacophore model. The obtained significant statistical parameters attested thepharmacophore model validity. The MLR and pharmacophore models are useful for the prediction of new insecticides with activity against Cowpea aphids.
Iranian Journal of Mathematical Chemistry
University of Kashan
2228-6489
10
v.
1
no.
2019
21
44
http://ijmc.kashanu.ac.ir/article_87360_33bb467a069e03051bd4af2f12de0824.pdf
dx.doi.org/10.22052/ijmc.2019.176522.1433
Energy of Signed Spongy Hypercubes
M.
Iranmanesh
Yazd University
author
M.
Saheli
Yazd University
author
text
article
2019
eng
A spongy hypercube is a Cartesian product of a d-connected polyhedral graph and a k-dimensional hypercube. The aim of this paper is to compute the energies of signed spongy hypercubes T□□(Q_k ) and O□□(Q_k ), where T and O are tetrahedron and octahedron, respectively.
Iranian Journal of Mathematical Chemistry
University of Kashan
2228-6489
10
v.
1
no.
2019
45
55
http://ijmc.kashanu.ac.ir/article_87362_66c02a1a62b5cbe1d4b5f98737c6b925.pdf
dx.doi.org/10.22052/ijmc.2019.159141.1409
On the Stability of Fullerenes
M. B.
Ahmadi
Department of Mathematics, Faculty of Sciences, Shiraz University
author
E.
Farhadi
Department of Mathematics, Faculty of Sciences, Shiraz University
author
M.
Ghavanloo
Department of Mathematics, Faculty of Sciences, Shiraz University
author
text
article
2019
eng
Fullerenes have wide application in various fields including electronic and optic, medical science, biotechnology and have received a lot of recent chemists and mathematicians’ attention. Due to many applications of fullerenes, the study of their stability is important. In this paper, we study the effective parameters that affect the fullerene's stability and then according to these parameters, we introduce a new function to examine the stability of every fullerene. By using this function, we determine the stable isometric of each fullerene in a unique way.
Iranian Journal of Mathematical Chemistry
University of Kashan
2228-6489
10
v.
1
no.
2019
57
69
http://ijmc.kashanu.ac.ir/article_87417_e285508bb371eba445b97f5c0b65b16c.pdf
dx.doi.org/10.22052/ijmc.2019.151000.1397
Aromaticity of fullerenes, the way to their functionalization (Review)
B.
Szefler
Department of Physical Chemistry, Faculty of Pharmacy,
Collegium Medicum, Nicolaus Copernicus University,
Kurpińskiego 5, Bydgoszcz 85-096, Poland
author
R.
Pop
University of Medicine and Pharmacy, Romania
author
text
article
2019
eng
Aromaticity is used to describe the durability and reactivity of structures containing delocalized electrons.In this review article, the aromaticity of fullerenes patched with flowers of 6-and 8-membered ringsis discussed, optimized at the HF and DFT levels of theory, in terms of HOMA and NICS criteria. The aromatic character of these nanostructures allows for functionalization and finally for increasing their solubility in polar solvents. The overall conclusion is that several of the yet hypothetical molecular nanostructures herein described are serious candidates for new medicinal products, as a proposal for personalized medicine.
Iranian Journal of Mathematical Chemistry
University of Kashan
2228-6489
10
v.
1
no.
2019
71
91
http://ijmc.kashanu.ac.ir/article_87580_d95a512ef99af03fb694424430d68f69.pdf
dx.doi.org/10.22052/ijmc.2019.174207.1430